Marked intrafamilial variability of clinical and neuroimaging manifestations in NFIB-related developmental disorder.

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Bibliographic Details
Title: Marked intrafamilial variability of clinical and neuroimaging manifestations in NFIB-related developmental disorder.
Authors: Gana S; Neurogenetics Research Center, IRCCS Mondino Foundation, Pavia, Italy., Serpieri V; Neurogenetics Research Center, IRCCS Mondino Foundation, Pavia, Italy., Giorgio E; Neurogenetics Research Center, IRCCS Mondino Foundation, Pavia, Italy.; Department of Molecular Medicine, University of Pavia, Pavia, Italy., Iorio M; Department of Brain and Behavioual Sciences, University of Pavia, Pavia, Italy., Rognone E; Advanced Imaging and Radiomics Center, Neuroradiology Department, IRCCS Mondino Foundation, Pavia, Italy., Pichiecchio A; Department of Brain and Behavioual Sciences, University of Pavia, Pavia, Italy.; Advanced Imaging and Radiomics Center, Neuroradiology Department, IRCCS Mondino Foundation, Pavia, Italy., Chiappedi M; Child Neurology and Psychiatry Unit, ASST Pavia, Vigevano, Italy., Valente EM; Neurogenetics Research Center, IRCCS Mondino Foundation, Pavia, Italy.; Department of Molecular Medicine, University of Pavia, Pavia, Italy.
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2023 May; Vol. 191 (5), pp. 1395-1400. Date of Electronic Publication: 2023 Feb 09.
Publication Type: Case Reports; Research Support, Non-U.S. Gov't; Journal Article
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Database: MEDLINE Ultimate
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